Canonical Allele Identifier: CA1980172822
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491137C= , CM000673.2:g.67491137C= GRCh38
NC_000011.9:g.67258608C= , CM000673.1:g.67258608C= GRCh37
NC_000011.8:g.67015184C= NCBI36
NG_008969.1:g.13104C= , LRG_460:g.13104C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*144C= ENSP00000507961.1:n.*144C=